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dc.contributor.author Bonta M
dc.contributor.author Hegedűs, Balázs
dc.contributor.author Limbeck A
dc.date.accessioned 2016-09-21T09:31:46Z
dc.date.available 2016-09-21T09:31:46Z
dc.date.issued 2016
dc.identifier.citation pagination=54-62; journalVolume=908; journalTitle=ANALYTICA CHIMICA ACTA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3667
dc.identifier.uri doi:10.1016/j.aca.2015.12.048
dc.description.abstract In this work, a novel calibration approach for minor and trace element quantification in LA-ICP-MS imaging of biological tissues is presented. Droplets of aqueous standard solutions are deposited onto pre-cut pieces of filter paper, allowed to dry, and sputtered with a thin gold layer for use as pseudo-internal standard. Analysis of the standards using LA-ICP-MS is performed using radial line-scans across the filters. In contrast to conventionally used preparation of matrix-matched tissue standards, the dried-droplet approach offers a variety of advantages: The standards are easy to prepare, no characterization of the standards using acid digestion is required, no handling of biological materials is necessary, and the concentration range, as well the number of investigated analytes is almost unlimited. The proposed quantification method has been verified using homogenized tissue standards with known analyte concentrations before being applied to a human malignant mesothelioma biopsy from a patient who had not received any chemotherapeutic treatment. Elemental distribution images were acquired at a lateral resolution of 40 mum per pixel, limits of detection ranging from 0.1 mug g(-1) (Mn, Ni, Cu, Zn) to 13.2 mug g(-1) (K) were reached.
dc.relation.ispartof urn:issn:0003-2670
dc.title Application of dried-droplets deposited on pre-cut filter paper disks for quantitative LA-ICP-MS imaging of biologically relevant minor and trace elements in tissue samples.
dc.type Journal Article
dc.date.updated 2016-09-20T13:48:49Z
dc.language.rfc3066 en
dc.identifier.mtmt 3076736
dc.identifier.pubmed 26826687
dc.contributor.department SE/AOK/I/IISZPI/MTA-SE Molekuláris Onkológia Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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